4,5-Dibromo-3-fluorothiophene-2-carboxylic acid

97%

Reagent Code: #177819
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CAS Number 1628447-64-2

science Other reagents with same CAS 1628447-64-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.93 g/mol
Formula C₅HBr₂FO₂S
badge Registry Numbers
MDL Number MFCD30183522
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and heterocyclic compounds. Its functional groups enable selective derivatization for building complex molecules. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the combined presence of bromine, fluorine, and carboxylic acid moieties on the thiophene ring. Also utilized in the preparation of organic semiconductors and specialty materials where halogenated thiophenes enhance electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,600.00
inventory 250mg
10-20 days ฿19,200.00
inventory 500mg
10-20 days ฿32,000.00
inventory 1g
10-20 days ฿48,000.00

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4,5-Dibromo-3-fluorothiophene-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and heterocyclic compounds. Its functional groups enable selective derivatization for building complex molecules. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the combined presence of bromine, fluorine, and carboxylic acid moieties on the thiophene ring. Also utilized in the preparation of organic semiconductors and specialty materials wh

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and heterocyclic compounds. Its functional groups enable selective derivatization for building complex molecules. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the combined presence of bromine, fluorine, and carboxylic acid moieties on the thiophene ring. Also utilized in the preparation of organic semiconductors and specialty materials where halogenated thiophenes enhance electronic properties.

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